NZ275100A

NZ275100A - Tetracyclic oxepine derivatives and medicaments

Info

Publication number: NZ275100A
Application number: NZ275100A
Authority: NZ
Inventors: Walter-Gunar Friebe; Werner Scheuer; Ulrich Tibes
Original assignee: Boehringer Mannheim Gmbh
Priority date: 1993-10-26
Filing date: 1994-10-22
Publication date: 1998-03-25
Also published as: AU8059494A; ATE157364T1; IL111412A; FI961780A; DE4336491A1; AU678638B2; EP0725784B1; ZA948366B; NO961657D0; NO961657L; FI961780A0; IL111412A0; TW293009B; HU219226B; ES2109019T3; HUT74071A; HU9601088D0; KR960705829A; US5696155A; CA2175070A1

Abstract

PCT No. PCT/EP94/03479 Sec. 371 Date Sep. 10, 1996 Sec. 102(e) Date Sep. 10, 1996 PCT Filed Oct. 22, 1994 PCT Pub. No. WO95/11906 PCT Pub. Date May 4, 1995Compounds of formula I <IMAGE> (I) in which Q denotes hydrogen, a hydroxy group or a C1 to C8 alkoxy group which can be substituted if desired, by carboxyl or C1 to C6 alkoxycarbonyl and either Y and Z together form a group <IMAGE> and X represents hydrogen, C1 to C6 alkyl or C2 to C6 alkenyl or Y and X together form a group <IMAGE>Z represents hydrogen, C1 to C6 alkyl or C1 to C6 alkanoyl, where R denotes hydrogen or a C1 to C6 alkyl residue as well as physiologically tolerated salts thereof, processes for their production and pharmaceutical agents containing these compounds for the treatment of inflammatory diseases and allergic diseases.

Description

<div class="application article clearfix" id="description"> New Zealand Paient Spedficaiion for Paient Number £75100 New Zealand No. 275100 International No. PCT/EP94/03479 TO BE ENTERED AFTER ACCEPTANCE AND PUBLICATION Priority dates: 26.10.1993; Complete Specification Filed: 22.10.1994 Classification:^) C07D493/04; A61K31/335.35 Publication date: 25 March 1998 Journal No.: 1426 Title of Invention: Dibenzo[b,e]oxepine derivatives, process for producing them and medicaments containing them Name, address and nationality of applicant(s) as in international application form: BOEHRINGER MANNHEIM GMBH, a German company of D-68298 Mannheim, Federal Republic of Germany NEW ZEALAND PATENTS ACT 1953 COMPLETE SPECIFICATION I. 275100 Boehringer Mannheim GmbH 3897/OO/WO Dibenz[b,e]oxepin derivatives, processes for their production and pharmaceutical agents which contain them The present invention concerns new dibenz[b,e]oxepin derivatives, processes for their production and pharmaceutical agents which contain these compounds. The invention concerns dibenz[b,e]oxepin derivatives of the general formula I X ° X V\v-- o - Y II T z d), o in which Q denotes hydrogen, a hydroxy group or a Cx to C8 alkoxy group which can be substituted if desired, by carboxyl or C: to C6 alkoxy-carbonyl and either Y and Z together form a group -C=CH-C0- and iooR 275100 - 2 - X represents hydrogen, C2 to C6 alkyl or C2 to C6 alkenyl or Y and X together form a group -C=CH-CO- or COOR an alkylene residue of 2 - 4 carbon atoms and Z represents hydrogen, C2 to C6 alkyl or C-j^ to C6 alkanoyl, where R denotes hydrogen or a C± to C6 alkyl residue as well as physiologically tolerated salts thereof. The compounds of formula I have valuable pharmacological properties, in particular they can inhibit the activity of phospholipases. They are therefore suitable for the treatment of acute and chronic, allergic, non-allergic and traumatic and inflammatory diseases such as rheumatoid arthritis, osteoarthritis, ulcerative colitis, acute pancreatitis, contact dermatitis, inflammatory and allergic respiratory tract diseases, septic shock, allergic shock, serum sickness, autoimmune diseases, graft-versus-host reactions, host-versus-graft diseases, ischaemic or thrombotic diseases such as coronary infarction or cerebral infarction. Alkyl residues in the said groups alkyl, alkoxy and alkanoyl can be straight-chained or branched. Preferred residues are the methyl, ethyl, propyl, isopropyl, n-butyl, isobutyl, tert.butyl, n-pentyl and 3-pentyl residues. 275100 3 Alkylene residues can be straight-chained or branched. Preferred residues are 1,2-ethylene, 1,3-propylene, 1,2-propylene and 1,4-butylene. Apart from the compounds mentioned in the examples, the invention also relates in particular to all substances which have any possible combination of the substituents mentioned in the examples. The process according to the invention for the production of compounds of formula I is characterized in that a compound of the general formula II in which Q has the above-mentioned meaning and one of the two residues and denotes acetyl whereas the other represents hydrogen, C2 to C5 alkyl or c2 to c6 alkenyl, is reacted in a known manner with an oxalic acid derivative such as for example diethyl oxalate under the influence of a base such as for example an alkali alcoholate and cyclized or a compound of the general formula III Q (ii), o 2751 - 4 - in which Q has the above-mentioned meaning and one of the two residues X2 and Z2 denotes hydrogen whereas the other represents hydrogen, Cx to C6 alkyl or C2 to C6 alkenyl, is reacted in a known manner with a halogenfumaric acid derivative such as for example bromofumaric acid dimethyl ester under the influence of a base such as for example an alkali alcoholate and cyclized, and subsequently, if desired, one or several of the residues Q, R, X and Z are converted into another residue given by the definition and/or converted into a physiologically tolerated salt. It is expedient to react compounds of formulae II and III in a basic medium such as a lower alcohol like methanol, ethanol or isopropanol in the presence of an alkali alcoholate. The subsequent cyclization is carried out for example in the presence of an acid such as sulphuric acid, polyphosphoric acid, polyphosphoric acid ester or alcoholic hydrochloric acid. In the case that Y and X together form an alkylene residue, the suitable compounds of formula II can be converted directly by acid catalysis into the corresponding compounds of formula I without the action of an oxalic acid derivative. A conversion of a residue Q into another residue Q defined by the claim is carried out for example by reacting a compound of formula I in which Q represents hydroxyl with an alkylation agent such as for example an alkyl halogenide which is substituted if desired. An alkoxy group representing Q can, if desired, be converted into a hydroxy group for example by cleaving a methoxy group with boron tribromide. 275100 - 5 - A carboxyl group can be produced by saponifying an alkoxycarbonyl group contained in Q or Y and Z or Y and X, and an alkoxycarbonyl group can be produced by esterifying a carboxyl group. If X represents an alkenyl residue then this can be converted, if desired, into an alkyl residue by hydrogenation. The starting compounds II and III are substances known in the literature or can be produced in analogy to processes known in the literature. Pharmacologically tolerated salts which come into consideration are in particular alkali, alkaline earth and ammonium salts and, if desired, salts with non-toxic inorganic or organic acids such as e.g. hydrochloric acid, sulphuric acid, phosphoric acid, hydrobromic acid, acetic acid, lactic acid, citric acid, malic acid, benzoic acid, salicylic acid, malonic acid, maleic acid, succinic acid or diaminocaproic acid. The salts are obtained in the usual manner for example by neutralizing the compounds of formula I with appropriate lyes or acids. In order to produce pharmaceutical agents, the compounds of the general formula I are mixed in a known manner with suitable pharmaceutical carrier substances, aroma substances, flavourings and dyes and are formed for example into tablets or coated tablets or are suspended or dissolved with the addition of appropriate auxiliary substances in water or oil such as e.g. olive oil. 27510 - 6 - The substances of the general formula I can be administered orally and parenterally in a liquid or solid form. Water is preferably used as the injection medium which contains the usual stabilizing agents, solubilizers and/or buffers for injection solutions. Such additives are for example tartrate or borate buffer, ethanol, dimethyl-sulfoxide, complexing agents (such as ethylene-diaminetetraace-ic acid), high molecular polymers (such as liquid polyethylene oxide) to regulate the viscosity or polyethylene derivatives of sorbitan hydrides. Solid carrier substances are e.g. starch, lactose, mannitol, methylcellulose, talcum, highly dispersed silicic acid, higher molecular polymers (such as polyethylene glycols). Suitable preparations for oral administration can if desired contain flavourings and sweeteners. For external application, the substances I according to the invention can also be used in the form of powders and ointments. For this they are for example mixed with powdery, physiologically tolerated diluents or conventional ointment bases. The administered dose depends on the age, health and weight of the recipient, the extent of the disease, the type of other treatments which may be carried out at the same time, the frequency of the treatments and the type of desired effect. The daily dose of the active compound is usually 0.1 to 50 mg/kg body weight. Normally 0.5 to 40 and preferably 1.0 to 20 nig/kg/day in one or several applications per day are effective in order to achieve the desired results. Apart from the substances mentioned in the examples, the - 7 - 27^ 10 0 following compounds are preferred within the scope of the invention: 1. 2-Carboxyinethoxy-7,13-dihydro-5H-10,12-dioxa- benzo[4,5]cyclohepta[1,2-b]naphthalen -5,7-dione-9-carboxylic acid-disodium 2. 7,12-Dihydro-5-propyl-lH-4,13-dioxabenzo[4,5]cyclohepta [ 1, 2-a] naphthalen-1,7-dione-3-carboxylic acid ethyl ester 3. ll-Allyl-7,13-dihydro-2-hydroxy-5H-10,12-dioxa-benzo[4,5]cyclohepta-[1,2-b]naphthalen- 5, 7-dione-9-carboxylic acid ethyl ester 4. ll-Allyl-7,l3-dihydro-2-ethoxycarbonylmethoxy-5H- 10,12-dioxabenzo[4,5]cyclohepta[l,2-b]naphthalen- 5, 7-dione -9-carboxylic acid ethyl ester 5. ll-Allyl-7,13-dihydro-2-octyloxy-5H-10,12-dioxa-benzo[4,5]cyclohepta[1,2-b]naphthalen-5,7-dione-carboxylic acid ethyl ester N.Z. PATENT OFFICE 0 9 OCT 1997 -.a~ 275 10 0 Example l 7.12-Dihvdro-lH-4.13-dioxabenzor 4.51cycloheptar1.2-a1 naphthalen-1,7-dione-3-carboxylic acid ethyl ester 8.04 g (30 mmol) 4-acetyl-6,ll-dihydro-3-hydroxy-dibenz[b,e]oxepin-ll-cne is added to a solution of 4.14 g (180 mmol) sodium in 2 50 ml ethanol, it is heated for 10 minutes to reflux, cooled to room temperature, admixed with 14.6 g (100 mmol) diethyl oxalate, heated for 90 minutes to reflux, allowed to cool and filtered. The precipitate is taken up in 100 ml ethanol, the suspension is saturated with hydrogen chloride and subsequently heated for 1 hour to 50°C. After cooling it is poured onto ice and filtered. 7.8 g of the title compound (74 % of theory) of melting point 178-180°C (from ethanol) remain. Example 2 The following are obtained in an analogous manner to that described in example 1: Name Yield % Melting point (solvent) a) 7,12-dihydro-10-hydroxy-lH-4,13-dioxabenzo[4,5]cyclohepta[1,2-a]-naphthalen— l, 7-dione-3-carboxylic acid-ethyl ester from 4-acetyl-6,ll-dihydro-3,8-dihydroxy-dibenz[b,e]oxepin-ll-one and diethyl oxalate 36 251-253 (diethyl ether) N.Z. p 09 OCT W97 R£CL 275 ^® - 9 - Name Yield % Melting point (solvent) b) 7,13-dihydro-5H-10,12-dioxabenzo-[4,5]cyclohepta[1,2-b]-naphthalen-5,7-dione-9-carboxylic acid ethyl ester from 2-acetyl-6,ll-dihydro-3-hydroxy-dibenz[b,e]oxepin-ll-one and diethyl oxalate 79 174-175 (ethanol) c) 7,13-dihydro-2-hydroxy-5H-10,12-dioxabenzo[4,5]cyclohepta[1,2-b]-naphthalen-5,7-dione-9-carboxylic acid ethyl ester from 2-acetyl-6,ll-dihydro-3 ,8-dihydroxy-dibenz[b,e] oxepin-ll-one and diethyl oxalate 77 210-212 (ethanol) d) 7,13-dihydro-ll-propyl-5H-10,12-dioxabenzo[4,5]cyclohepta[l,2-b]-naphthalen-5,7-dione-9-carboxylic acid ethyl ester from 2-acetyl-6,11-dihydro-3-hydroxy-4-propyl-dibenz[b,e]oxepin-ll-one and diethyl oxalate 84 194-196 (ethanol) e) ll-allyl-7,13-dihydro-5H-10,12-dioxabenzo[4,5]cyclohepta[1,2-b]-naphthalen-5,7-dione-9-carboxylic acid ethyl ester from 2-acetyl-4-allyl-6,ll-dihydro-3-hydroxy-dibenz[b,e]oxepin-ll-one and diethyl oxalate 79 179-181 (ethanol) - 10 - 275100 Name Yield % Melting point (solvent) f) 7,13-dihydro-2-hydroxy-ll-propyl-5H-10,12-dioxabenzo-[4,5]cyclohepta-.1, 2-b] naphthalen-5, 7-dione-9-carboxylic acid ethyl ester from 2-acetyl-6,ll-dihydro-3 ,8-dihydroxy-4-propyl-dibenz [b,e] -oxepin-ll-one and diethyl oxalate 91 265-268 (ethanol) g) 7,l3-dihydro-2-methoxy-ll-propyl-5H- 10,12-dioxabenzo[4,5]cyclo-hepta [1,2-b]naphthalen-5,7-dione-9-carboxylic acid ethyl ester from 2-acetyl-6,ll-dihydro-3-hydroxy-8- methoxy-4-propyl-dibenz[b,e]oxepin- ll-one and diethyl oxalate 87 182-183 (ethanol) h) ll-allyl-7,13-dihydro-2-methoxy-5H-10,12-dioxabenzo[4,5]cyclo-hepta [1,2-b]naphthalen-5,7-dione-9-carboxylic acid ethyl ester from 2-acetyl-4-allyl-6,ll-dihydro-3-hydroxy-8-methoxy-dibenz[b,e]-oxepin-ll-one and diethyl oxalate 84 156-158 (ethanol) i) 7,l3-dihydro-2-methoxy-5H-10,12-dioxabenzo [4,5]cyclohepta[1,2-b]-naphthalen-5,7-dione-9-carboxylic acid ethyl ester from 2-acetyi-6,ll-dihydro-3-hydroxy-8-methoxy-dibenz[b,e]oxepin-ll-one and diethyl oxalate 78 223-225 (ethanol) j) 7,l2-dihydro-10-methoxy-lH-4,13-dioxabenzo[4,5]cyclohepta[1,2-a]-naphthalen-1,7-dione-3-carboxylic acid ethyl ester from 4-acetyl-6,il-dihydro-3-hydroxy-4-methoxy-dibenz[b,e]oxepin-ll-one and diethyl oxalate 76 183-185 (ethanol) 09 OCT 1997 - 11 - 27 5 1 0 0 Example 3 7.13-Dihvdro-2-octvloxv-5H-10.12-dioxabenzor 4.51- cyclohepta[1,2-b]naphthalen-5,7-dione-9-carboxylic acid ethvl ester A mixture of 3.7 g (10 mmol) of the compound of example 2c, 50 ml dimethylformamide, 1.4 g potassium carbonate and 1.75 ml 1-bromooctane is heated for 6 hours to 80°C, subsequently filtered and the filtrate is concentrated by evaporation. It is taken up in ethyl acetate and chromatographed on silica gel (eluting agent: ethyl acetate : isohexane 1:1). After trituration with ether, 2.4 g of the title compound (50 % of theory) remains of melting point 103-105°C. Example 4 The following are obtained in an analogous manner to that described in example 3: Name Melting point (solvent) a) 7,13-dihydro-2-octyloxy-ll-propyl- 63 5H-10,12-dioxabenzo-[4,5]cyclohepta [1,2-u]naphthalen-5,7-dione-9-carboxylic acid ethyl ester from the compound of example 2f and octylbromide (ether) 90-91 b) 7,13-dihydro-2-ethoxycarbonyl-methoxy-5H-10,12-dioxabenzo-[4,5]cyclohepta[1,2-b]naphthalen-5,7-dion.e-9-carboxylic acid ethyl ester from the compound of example 2c and bromoacetic acid ethyl ester 86 190-192 (ether) - 12 - 275100 7,13-dihydro-2-ethoxycarbonyl-methoxy-ll-propyl-5H-10,12-dioxabenzo [4,5]eyelohepta[1,2-b]-naphthalen-5,7-dione-9-carboxylic acid ethyl ester from the compound of example 2f and bromoacetic acid ethyl ester 151-152 (ethanol) Example 5 7.13-Dihvdro-5H-10.12-dioxabenzo r 4.51cyclohepta [1,2-b]naphthalen-5,7-dione-9-carboxylic acid-sodium 19 ml N sodium hydroxide solution and 3 0 ml water are added to a solution of 6.65 g (19 mmol) of the compound of example 2b in 150 ml ethanol, it is heated for 30 minutes to 70°C, allowed to cool and the precipitate is filtered. 5.2 g of the title compound (80 % of theory) is obtained with a decomposition point above 290°C. Example 6 The following are obtained in an analogous manner to that described in example 5: Name Yield Melting point (solvent) 7,13-dihydro-2-hydroxy-5H-10,12-dioxabenzo- [4, 5]cyclohepta[l,2-b]-naphthalen-5,7-dione-9-carboxylic acid sodium from the compound of example 2c 67 above 280 (water) N.Z. PATCNT C 09 OCT 1997 - 13 - 27 5 ^ 0 0 b) 7,13-dihydro-2-octyloxy-5H-10,12-dioxabenzo [4,5]cyclohepta[1,2-b]-naphthalen-5,7-dione-9-carboxylic acid sodium from the compound of example 3 88 above 280 (water) c) 7,13-dihydro-2-ethoxycarbonyl-raethoxy-5H-10,12-dioxabenzo[4,5]-cyclohepta[1,2-b]-naphthalen-5,7-dione-9-carboxylic acid sodium from the compound of example 4b 56 above 280 (water) d) 7,13-dihydro-2-methoxy-5H-10,12-dioxabenzo [4,5]cyclohepta[1,2-b]-naphthalen-5,7-dione-9-carboxylic acid sodium from the compound of example 2i 47 above 280 (water) e) 7,12-dihydro-lH-4,13-dioxabenzo-[4,5]cyclohepta[1,2-a]-naphthalen-1,7-dione-3-carboxylic acid sodium from the compound of example 1 75 above 280 (water) f) 7,12-dihvdro-l0-methoxy-lH-4,13-dioxabenzo[4,5]cyclohepta[1,2-a]-naphthalen-l,7-dione-3-carboxylic acid sodium from the compound of example 2j 52 above 280 (water) Example 7 4-Acetvl-9-methoxv-2-methyl-l.2.6.ll-tetrahvdro-3.12-dioxabenzo f 4.51cyclohepta r1.2-elinden-6-one 3.9 g (11 mmol) 2-acetyl-4-allyl-6,ll-dihydro-3-hydroxy-8-methoxy-dibenz[b,e]oxepin-ll-one is added at 100°C to a mixture of 9.2 g phosphorus pentoxide and 6 ml ethanol, heated for 30 minutes to 140°C, poured N.Z. PAi ENT OFF onto icr 0 9 OCT 1997 275100 and filtered. After chromatography on silica gel (eluting agent: ethyl acetate: isohexane 1:1) 0.9 g of the title compound (23 % of theory) of malting point 159-160°C (from ether) is isolated. 5-Acetyl-7,12-dihydro-l0-methoxy-lH-4,13-dioxa-benzo[4,5]cyclohepta[l,2-a]naphthalen-7-one can be detected as a by-product. Example 8 Inhibition of PLA2 activity The human recombinant type II PLA2 (= synovial PLA2) as a typical representative of a PLA2 was used for the test. The table shows the percentage in-vitro inhibition of this enzyme by the model compounds of examples 2a), 2c) and 4a) . The enzyme was inhibited dose-dependently and 78.61 and 49 % inhibition was already achieved with 10 Mg/ml« In contrast the table shows that although indomethacin also inhibited the enzyme, the maximum inhibition was only 52 % at the highest concentration of 100 jug/ml. This documents the superiority of the new sPLA2 inhibitors compared to a cyclooxygenase inhibitor. </div>

Claims

<div class="application article clearfix printTableText" id="claims"> 2751 - 15 - Table: Inhibition of the sPLA2 enzyme activity by tetracyclic dibenzoxepin derivatives and indomethacin Substances Concentrations Ex.2c) Ex.2a) Ex.4a) Indomethacin 100 jug/ml n.d. n.d. n.d. 52 10 nq/ml 78 61 49 10 1 /xg/ml 73 52 17 0 0.1 jLtg/ml 12 28 16 n.d Means of 3 experiments (duplicate determinations), n.d.= not determined 275100 Claims Dibenz[b,e]oxepin derivatives of formula I X in which Q denotes hydrogen, a hydroxy group or a Cx to c8 alkoxy group which can be substituted if desired, by carboxyl or Cx to C6 alkoxycarbonyl and either Y and Z together form a group -C=CH-C0- and iooR X represents hydrogen, C1 to C6 alkyl or C2 to C5 alkenyl or Y and X together form a group -C=CH-CO- or COOR an alkylene residue of 2 - 4 carbon atoms and Z represents hydrogen, C2 to c6 alkyl or Cx to c6 alkanoyl, where - 17 - 275100 R denotes hydrogen or a C: to C6 alkyl residue as well as physiologically tolerated salts .hereof. Process for the production of dibenz[b,e]oxepin derivatives of formula I in which Q denotes hydrogen, a hydroxy group or a C1 to c8 alkoxy group which can be substituted if desired, by carboxyl or a C± to C6 alkoxycarbonyl and either Y and Z together form a group -C=CH-C0- and COOR X represents hydrogen, Cx to c5 alkyl or c2 to C6 alkenyl or Y and X together form a group -C=CH-CO- or COOR an alkylene residue of 2 - 4 carbon atoms and Z represents hydrogen, Cx to c6 alkyl or Cx to c5 X o 18 275100 alkanoyl, where R denotes hydrogen or a C1 to C5 alkyl residue as well as physiologically tolerated salts thereof, wherein in a known manner in which Q has the above-mentioned meaning and one of the two residues Xi and Z1 denotes acetyl whereas the other represents hydrogen, C1 to C6 alkyl or C2 to C6 alkenyl, is reacted with an oxalic acid derivative such as for example diethyl oxalate under the influence of a base such as for example an alkali alcoholate and cyclized a) a compound of formula II (II) , O or b) a compound of the general formula III O-H *2 (III) O - 19 - 275 1° 0 in which Q has the above-mentioned meaning and one of the two residues X2 and Z2 denotes hydrogen whereas the other represents hydrogen, Cx to C6 alkyl or C2 to C6 alkenyl is reacted with a halogenfumaric acid derivative such as for example bromofumaric acid dimethyl ester under the influence of a base such as for example an alkali alcoholate and cyclized and subsequently, if desired, one or several of the residues Q, R, X and Z are converted into another residue given by the definition and/or converted into a physiologically tolerated salt. 

3. Pharmaceutical agent containing at least one compound as claimed in claim 1 in addition to the usual carrier and auxiliary substances. 

4. Use of compounds as claimed in claim 1 for the production of pharmaceutical agents for the treatment of acute and chronic, allergic, non-allergic and traumatic and inflammatory diseases. 

5. A compound of the formula (I) according to claim 1 substantially as herein described or exemplified. 

6. A process according to claim 2 substantially as herein described of exemplified. 

7. A pharmaceutical agent according to claim 3 substantially as herein described or exemplified. 

8. Use according to claim 4 substantially as herein described or exemplified. END OF C'-AlMS N.
2. PATENT OFFICE 0 9 OCT 1997 </div>